30 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
6400 Ultrasound System,7400 Ultrasound System, 7410 Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML)
FDA 510(k)
FDA Class 2
·General Hospital
DENSHIELD TREATMENT FOR SENSITIVE TEETH
FDA 510(k)
FDA Class 2
·Dental
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·November 10, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·April 11, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·March 15, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·June 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 10, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·March 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 16, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·January 26, 2018
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2014
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 13, 2011
PROLENE POLYPROPYLENE MESH
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·June 11, 2013
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 6, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 3, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·January 10, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 16, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·June 6, 2018